Product Details

SNP ID

rs104894742

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:67545150 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGATTCAGCCAAGCTCAAGGATG[A/G]AAGTGCAGTTAGGGCTGGGAAGGGT

Phenotype

MIM: 313700

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

AR PubMed Links

Gene Details

Gene

AR

Gene Name

androgen receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000044.3	1119	Missense Mutation	AAA,GAA	K2E	NP_000035.2
NM_001011645.2	1119	Intron			NP_001011645.1

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